Sticht Center on Aging, Department of Internal Medicine, Section on Gerontology and Geriatric Medicine, Wake Forest School of Medicine, Winston-Salem, NC 27157, USA.
J Gerontol A Biol Sci Med Sci. 2012 Oct;67(10):1099-106. doi: 10.1093/gerona/gls077. Epub 2012 Mar 26.
Obesity-related increases in multiple inflammatory markers may contribute to the persistent subclinical inflammation common with advancing age. However, it is unclear if a specific combination of markers reflects the underlying inflammatory state. We used factor analysis to identify inflammatory factor(s) and examine their associations with adiposity in older adults at risk for disability.
Adiponectin, CRP, IL-1ra, IL-1sRII, IL-2sRα, IL-6, IL-6sR, IL-8, IL-15, sTNFRI, sTNFRII, and TNF-α were measured in 179 participants from the Lifestyle Interventions and Independence for Elders Pilot (Mean ± SD age 77 ± 4 years, 76% white, 70% women). Body mass index, waist circumference, and total fat mass were assessed by anthropometry and dual-energy x-ray absorptiometry.
IL-2sRα, sTNFRI, and sTNFRII loaded highest on the first factor (factor 1). CRP, IL-1ra, and IL-6 loaded highest on the second factor (factor 2). Factor 2, but not factor 1, was positively associated with 1-SD increments in waist circumference (β = 0.160 ± 0.057, p = .005), body mass index (β = 0.132 ± 0.053, p = .01), and total fat mass (β = 0.126 ± 0.053, p = .02) after adjusting for age, gender, race/ethnicity, site, smoking, anti-inflammatory medications, comorbidity index, health-related quality of life, and physical function. These associations remained significant after further adjustment for grip strength, but only waist circumference remained associated with inflammation after adjusting for total lean mass. There were no significant interactions between adiposity and muscle mass or strength for either factor.
Greater total and abdominal adiposity are associated with higher levels of an inflammatory factor related to CRP, IL-1ra, and IL-6 in older adults, which may provide a clinically useful measure of inflammation in this population.
与肥胖相关的多种炎症标志物的增加可能导致与年龄增长相关的持续亚临床炎症。然而,目前尚不清楚是否存在特定的标志物组合可以反映潜在的炎症状态。我们使用因子分析来确定炎症因子,并研究它们与有残疾风险的老年人的肥胖之间的关系。
在 179 名来自生活方式干预和老年人独立试验的参与者中测量了脂联素、CRP、IL-1ra、IL-1sRII、IL-2sRα、IL-6、IL-6sR、IL-8、IL-15、sTNFRI、sTNFRII 和 TNF-α(平均±SD 年龄 77±4 岁,76%为白人,70%为女性)。通过人体测量学和双能 X 射线吸收法评估体重指数、腰围和总脂肪量。
IL-2sRα、sTNFRI 和 sTNFRII 在第一个因子(因子 1)上的负荷最高。CRP、IL-1ra 和 IL-6 在第二个因子(因子 2)上的负荷最高。调整年龄、性别、种族/民族、地点、吸烟、抗炎药物、合并症指数、健康相关生活质量和身体功能后,因子 2(但不是因子 1)与腰围(β=0.160±0.057,p=0.005)、体重指数(β=0.132±0.053,p=0.01)和总脂肪量(β=0.126±0.053,p=0.02)的 1-SD 增量呈正相关。在进一步调整握力后,这些相关性仍然显著,但在调整总瘦体重后,只有腰围与炎症相关。在两个因子中,肥胖与肌肉质量或力量之间没有显著的相互作用。
在老年人中,更高的总体和腹部肥胖与与 CRP、IL-1ra 和 IL-6 相关的炎症因子水平更高相关,这可能为该人群提供一种有用的炎症临床测量方法。